A concise synthesis of (±)-3-deoxyisoaltholactone
2014
Fearnley, Stephen Philip | Lory, Pedro
The novel styryl lactone analog (±)-3-deoxyisoaltholactone was synthesized in 5 steps from dihydrofuran. An intramolecular vinylsilane–oxocarbenium condensation thus afforded the central cis-fused bicyclic ether array in near quantitative yield as a single stereoisomer.
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Библиографическая информация
Tetrahedron letters
Том
55
Выпуск
37
Нумерация страниц
5207
- 5209
ISSN
0040-4039
Издатель
Elsevier Ltd
Другие темы
Oxocarbenium; Styryl lactone; Vinylsilane; Isoaltholactone; Cis-fused ether array; Stereoisomers
Язык
Английский
Тип
Journal Article; Text
2024-02-28
MODS
Поставщик данных
Эту запись предоставил National Agricultural Library
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